ARTEMA AQUA+ N— 510(k) K912335

Substantially Equivalent

Artema Medical AB

FDA 510(k) clearance K912335 for ARTEMA AQUA+ N, Substantially Equivalent on 1991-07-26. Applicant: Artema Medical AB.

Clearance details

Applicant: Artema Medical AB
Product code: Code BYD
Advisory panel: Anesthesiology
Date received: 1991-05-24
Decision date: 1991-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sweden, SE

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